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Page 1
Novel KCNV2 mutations in cone dystrophy with supernormal rod electroretinogram.
Ben Salah S, Kamei S, Sénéćhal A, Lopez S, Bazalgette C, Bazalgette C, Eliaou CM, Zanlonghi X, Hamel CP. Ben Salah S, et al. Among authors: eliaou cm. Am J Ophthalmol. 2008 Jun;145(6):1099-106. doi: 10.1016/j.ajo.2008.02.004. Epub 2008 Apr 9. Am J Ophthalmol. 2008. PMID: 18400204
Mutations in RPE65 cause Leber's congenital amaurosis.
Marlhens F, Bareil C, Griffoin JM, Zrenner E, Amalric P, Eliaou C, Liu SY, Harris E, Redmond TM, Arnaud B, Claustres M, Hamel CP. Marlhens F, et al. Nat Genet. 1997 Oct;17(2):139-41. doi: 10.1038/ng1097-139. Nat Genet. 1997. PMID: 9326927 No abstract available.
[Cavitary choroidal melanoma in a child].
Faraj H, Levy-Gabriel C, Lumbroso-Le Rouic L, Chefchaouni MC, Langmann ME, Orbach D, Sastre X, Couturier J, Eliaou CM, Desjardins L. Faraj H, et al. Among authors: eliaou cm. J Fr Ophtalmol. 2006 May;29(5):559-63. doi: 10.1016/s0181-5512(06)73811-6. J Fr Ophtalmol. 2006. PMID: 16885832 French.